Characterization of sediment toxicity in Shanghai Harbor using toxicity tests and digital gene expression analysis based on clams Ruditapes phillipinarum

Liru Liu; Jingjing Miao; Luqing Pan; Zhen Li; Yawei Sun

doi:10.1016/j.ecoenv.2020.111065

Characterization of sediment toxicity in Shanghai Harbor using toxicity tests and digital gene expression analysis based on clams Ruditapes phillipinarum

Ecotoxicol Environ Saf. 2020 Nov:204:111065. doi: 10.1016/j.ecoenv.2020.111065. Epub 2020 Aug 9.

Authors

Liru Liu¹, Jingjing Miao², Luqing Pan¹, Zhen Li¹, Yawei Sun³

Affiliations

¹ The Key Laboratory of Mariculture, Ministry of Education, Ocean University of China, Qingdao, 266003, PR China.
² The Key Laboratory of Mariculture, Ministry of Education, Ocean University of China, Qingdao, 266003, PR China. Electronic address: jmiao@ouc.edu.cn.
³ East China Sea Monitoring Center, State Oceanic Administration, Shanghai, 200137, PR China.

PMID: 32784014
DOI: 10.1016/j.ecoenv.2020.111065

Abstract

In the present study, chemical analysis of contaminants (three classes of organic pollutants and seven metals) and elutriate toxicity test were adopted to evaluate the potential environmental hazards of dredged sediment samples from five sites (SS1-5) along Huangpu River Channel (Shanghai Harbor, China). The metal Pb, Cu, Cr, Zn and the organic pollutants including total hexachlorocyclohexane (HCHs) and total dichlorodiphenyltrichloroethane (DDTs) in the five samples exceeded the threshold for effects level (TEL) to varying degrees. The probable effect concentration quotients (Q_PECm) of contaminants from the five dredged samples were all above 0.25, which means potential toxicity risks. Elutriate toxicity tests using medaka fish (Oryzias melastigma) and manila clam (Ruditapes philippinarum) showed that SS2 caused mortality to both species and SS1 caused mortality to fish. To explore the molecular biomarkers that may reflect the toxic effects, differential expressed genes were identified by RNA-Seq-based transcriptome profiling from the survived clams exposed to the two polluted elutriates (SS1, SS2). In clams exposed to SS1 and SS2 elutriate, 368 and 860 differential expressed genes (DEGs) were up-regulated, 199 and 1304 genes were down-regulated, respectively. Fourteen DEGs were selected from the enriched pathways that reflect cytotoxicity and responses to xenobiotics for the following quantitative real time PCR analysis. The transcriptomic profiling and the selected gene's expression patterns from clams exposed to SS1 and SS2 showed significant differences with the non-contaminated and control groups. Using the expression data of the selected gene battery in Factor Analysis allowed the discrimination between contaminated and non-contaminated sites and may reflect an influence gradient of sites. The development of the assay of these molecular biomarkers may provide a rapid and high-throughput tool for the quality assessment of the dredging sediments.

Keywords: Dredging sediment; Gene expression; Ruditapes philippinarum; Toxicity test; Transcriptomic.

MeSH terms

Animals
Bivalvia / drug effects*
Bivalvia / genetics
China
DDT / toxicity
Environmental Monitoring / methods*
Gene Expression / drug effects*
Geologic Sediments / chemistry*
Hexachlorocyclohexane / toxicity
Metals, Heavy / toxicity
Rivers / chemistry*
Toxicity Tests
Water Pollutants, Chemical / toxicity*

Substances

Metals, Heavy
Water Pollutants, Chemical
Hexachlorocyclohexane
DDT